Variant report

Variant	rs7668393
Chromosome Location	chr4:30715601-30715602
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10003328	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10005883	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10939311	0.90[ASN][1000 genomes]
rs13105058	0.94[ASN][1000 genomes]
rs1486767	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6448718	0.90[ASN][1000 genomes]
rs9918044	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30713000-30718400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:30713200-30717800	Weak transcription	Aorta	Aorta
3	chr4:30714800-30715800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:30714800-30715800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:30714800-30716000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr4:30714800-30717600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr4:30714800-30717800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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